Canonical Allele Identifier: PA2580136679
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 2185522
ClinVar RCV Id: RCV002596189 RCV002596188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Leu126Val
CA8288907
NM_001128085.1:c.376C>G